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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K151374

NuVasive MLX-Medial Lateral Expandable Lumbar Interbody System, NuVasive AP Expandable XLIF System · Nu Vasive, Incorporated · decided 2015-08-06 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
APX1672353Nuvasive, Inc.MAX PHM00887517454041
MLX2103424Nuvasive, Inc.MAX PHM00887517263841
MLX3321716Nuvasive, Inc.MAX PHM00887517498267
APX1672380Nuvasive, Inc.MAX PHM00887517454003
MLX4103828Nuvasive, Inc.MAX PHM00887517265364
MLX2083424Nuvasive, Inc.MAX PHM00887517263087
MLX2083828Nuvasive, Inc.MAX PHM00887517263094
MLX1642460Nuvasive, Inc.MAX PHM00887517700100
MLX1642466Nuvasive, Inc.MAX PHM00887517700162
MLX4080008Nuvasive, Inc.MAX PHM00887517729293
MLX8083828Nuvasive, Inc.MAX PHM00887517268129
APX1672391Nuvasive, Inc.MAX PHM00887517184764
MLX3321715Nuvasive, Inc.MAX PHM00887517498250
MLX1642465Nuvasive, Inc.MAX PHM00887517700155
MLX8103424Nuvasive, Inc.MAX PHM00887517268174
MLX4080012Nuvasive, Inc.MAX PHM00887517732637
MLX8123424Nuvasive, Inc.MAX PHM00887517268938
MLX4083424Nuvasive, Inc.MAX PHM00887517264497
APX1632872Nuvasive, Inc.MAX PHM00887517210593
APX1672392Nuvasive, Inc.MAX PHM00887517454072
MLX4103424Nuvasive, Inc.MAX PHM00887517265357
APX1672343Nuvasive, Inc.MAX PHM00887517451590
APX1632870Nuvasive, Inc.MAX PHM00887517210579
MLX3321703Nuvasive, Inc.MAX PHM00887517498137
MLX4080010Nuvasive, Inc.MAX PHM00887517732613